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Thy1.1 mice

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Thy1.1 mice are a strain of laboratory mice commonly used in research. They express the Thy1.1 allele, which is a genetic marker often used to identify and isolate specific cell types. The core function of Thy1.1 mice is to serve as a tool for researchers to study various aspects of immunology, cell biology, and related fields.

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15 protocols using thy1.1 mice

1

Murine Models for Immunological Studies

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C57BL/6 and BALB/c mice (6–8 week-old and male weighing 20 ± 3 g) were purchased from Guangdong Medical Laboratory Animal Center (Guangzhou, Guangdong, China) while IL-10–/– and Thy1.1+ mice in a C57BL/6 background were purchased from the Jackson Laboratory (Bar Harbor, ME). All mice were housed in specific pathogen-free rooms with controlled conditions. All experiments were approved by the Institutional Animal Ethical Committee of Guangdong Provincial Academy of Chinese Medical Sciences.
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2

Cxxc1 Conditional Knockout Mice

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C57BL/6 mice were purchased from CLEA. Cxxc1fl/fl mice were established by Haruhiko Koseki (Brown et al., 2017 (link)) and backcrossed at Chiba University to a C57BL/6 background 10 times. Cxxc1fl/fl mice were crossed with Rosa26-Cre-ERT mice (TaconicArtemis), OT-II TCR Tg mice, and Thy1.1 mice (The Jackson Laboratory). OT-II TCR Tg mice express TCRs specific for residues 323–339 of the OVA protein. All mice used in this study were maintained under specific pathogen–free conditions and ranged from 6 to 8 wk of age. The protocols of all of the animal experiments were approved by the Chiba University animal committee. All mice used in this study were female. All animal care was performed in accordance with the guidelines of Chiba University. The research proposals were reviewed by the ethics committee for animals at Chiba University (registration numbers 1-254 and 1-300).
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3

Generation of OVA-specific TCR-αβ Transgenic Mice

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OVA-specific TCR-αβ (DO11.10) transgenic (Tg) mice were provided by Dr. D. Loh (Washington University School of Medicine, St. Louis), and backcrossed to BALB/c mice ten times56 (link). BALB/c, BALB/c nu/nu and C57BL/6 mice were purchased from CLEA Japan. Thy1.1 mice with a BALB/c background were purchased from Jackson Laboratories. NSG mice were purchased from Charles river laboratories. All mice were used at 6–8 weeks old and were maintained under specific pathogen-free conditions. Animal care was conducted in accordance with the guidelines of Chiba University.
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4

Genetic Mouse Models of Pancreatic Cancer

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KrasLSL-G12D/+;Trp53L/+;Pdx1-Cre;Rosa26YFP/YFP and KrasLSL-G12D/+;Trp53LSL-R172H/+;Pdx1-Cre;Rosa26YFP/YFP (KPCY) mice have been previously described (Rhim et al., 2012 (link)), and were bred and maintained under two pathogen-free facilities at the University of Pennsylvania. Specifically, KrasLSL-G12D/+;Trp53L/+;Pdx1-Cre;Rosa26YFP/YFP mice were used for Figure 1C to quantify the CD3+ T cell infiltration in a group of primary KPCY tumors. KrasLSL-G12D/+;Trp53LSL-R172H/+;Pdx1-Cre;Rosa26YFP/YFP (KPCY) mice were used for all other experiments in this manuscript. All wild-type C57BL/6, NOD/SCID, Batf3−/−, CXCR2+/−. CXCR2−/−, and Thy1.1+ mice were purchased from The Jackson Laboratory and/or bred at the University of Pennsylvania. All animal procedures were conducted following National Institutes of Health guidelines. Animal protocols were reviewed and approved by the Institute of Animal Care and Use Committee at the University of Pennsylvania.
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5

Breeding and Sourcing of Mouse Strains

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C57/BL6 mice were obtained from Jackson Laboratories, bred in-house, and bred off-site at Charles River. Foxp3-RFP reporter mice (C57BL/6-Foxp3tm1Flv/J), Foxp3-Ametrine reporter (C57BL/6.Foxp3flpo-mAmetrine), and RAG1 knockout (C57BL/6-Rag1tm1Mom/J) mice were bred in-house and off-site at Charles River. Foxp3Cre-ERT2.GFP × Rosa26LSL.Td.Tomato mice were bred in-house. Thy1.1 mice were obtained from Jackson Laboratories. Mice used in experiments were male and female between 6 and 10 wk old at the initiation of the study. All animal work and protocols in this study were approved by the University of Pittsburgh Institutional Animal Care and Use Committee, accredited by the Association for Assessment and Accreditation of Laboratory Animal Care.
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6

Generation of HMPV-infected Mice Models

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C57BL/6 (B6) and congenic Thy1.1+ mice were purchased from Jackson Laboratory. B6-Kb0Db0;B7.2 transgenic (B7tg) mice were obtained with permission from Drs. Alexander Sette (La Jolla Institute for Allergy and Immunology, La Jolla, CA) and Francois Lemonnier (Institut Pasteur, Paris, France). PD-1−/− mice were obtained with permission from Dr. Tasuku Honjo (Kyoto University, Kyoto, Japan). All animals were bred and maintained in specific pathogen-free conditions in accordance with the Vanderbilt Institutional Animal Care and Use Committee. 6-12 week old age- and gender-matched animals were used in all experiments. Mixed bone-marrow chimeric mice were generated by irradiating Thy1.1+ recipients with 2 doses of 5 Gy, 4 hours apart, followed by reconstitution with 1×106 WT (Thy1.1+) and 1×106 PD-1−/− (Thy1.2+) bone-marrow cells 24 hours later. Mice were rested for 8 weeks and then bled to check reconstitution before use in experiments. HMPV (pathogenic clinical strain TN/94-49, genotype A2) was grown and titered in LLC-MK2 cells as previously described (31 (link)). For all experiments, mice were anesthetized with ketamine-xylazine and infected intranasally (i.n.) with 1×106 PFU of HMPV.
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7

Mouse Models for Immunological Research

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Wild-type mice and Rag1−/− mice were purchased from Shanghai SLAC Laboratory Animal Co. Thy1.1 mice were purchased from Jackson laboratory. Rag2−/−Il2rg−/− mice were purchased from Taconics. Il17e−/− (B6; 129S5-Il25tm1Lex/Orl) mice were purchased from EMMA. Rorcgfp/gfp50 (link) , MyD88−/− 56 (link) and Ahr−/− mice 57 (link) and IL-17A-GFP reporter mice 58 (link) were generated previously. IL-17-deficient mouse was kindly provided by Dr. Hong Tang (Institute Pasteur of Shanghai, Chinese Academy of Science). All mice used in this study are on C57BL/6 background and maintained in specific pathogen-free conditions. All mice used in the experiments were 6–10 weeks old. Gender-matched male and female mice were used in the study. In IL-33-induced lung inflammation, in which BALF (bronchoalveolar lavage fluids) cells were analyzed, littermate female mice were used. All animal experiments were performed in compliance with the guide for the care and use of laboratory animals and were approved by the institutional biomedical research ethics committee of the Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences.
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8

Establishing T-cell-specific Pgam1 Knockout Mice

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CD4-Cre transgenic (TG) mice, OT-1 Tg mice, Thy1.1+ mice, and Thy1.2+ mice were purchased from The Jackson Laboratory (Bar Harbor, ME, USA). Pgam1flox/flox mice were kindly provided by Drs. Hiroshi Kondoh and Takumi Mikawa (Kyoto University). In brief, the exon 2–4 of pgam1 was pinched by two loxP sequences, and FLP-flanked neo-cassette was inserted in the 5′ upstream region of exon 2 to generate the pgam1 targeting vector. Targeting vector was injected into C57BL/6 mouse embryonic stem cells. The founder mice were crossed with FLP transgenic mice to remove the neo-cassette gene to generate Pgam1-floxed mice. Pgam1-floxed mice were crossed with CD4-Cre TG mice to generate T-cell-specific Pgam1-deficient mice. Gene-manipulated mice with a C57BL/6 background were used in all experiments. These mice were purchased from Clea Japan, Inc. (Tokyo, Japan). Both male and female mice were used in the experiments. All mice were used at 8–12 weeks of age.
All of the animal experiments received approval from the Ehime University Administrative Panel for Animal Care. All animal care was conducted in accordance with the guidelines of Ehime University. All experiments using Lm-OVA were performed in accordance with the protocols approved by the Ehime University Institution Biosafety Committee.
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9

Mouse Strains for Immunological Studies

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C57BL/6 (WT) mice were obtained from Charles River Laboratories. CCR2-RFP, Actin-eGFP, IL12p40-eYFP, Il12b−/−, ifngr1−/−, LysMcre, Csf1rLsL-DTR, Ccr7−/−, OTII (male-linked) and Thy1.1 mice were obtained from Jackson Laboratories. Ifnar−/− mice (Müller et al., 1994 (link)), were a gift from Michel Aguet (University of Zurich, Zurich, Switzerland). REX3-Tg mice were generated by our lab as previously described (Groom et al., 2012 (link)). Kaede transgenic mice were obtained from Dr. Osami Kanagawa (RIKEN Institute) (Tomura et al., 2008 (link)), rederived at Taconic and then bred at Massachusetts General Hospital. LysMcre mice were crossed with Csf1rLsL-DTR to generate MM-DTR mice as previously described (Schreiber et al., 2013 (link)). All mice were maintained on the C57BL/6 background. REX3-Tg and IL12p40-eYFP mice were bred and maintained in specific pathogen free (SPF) plus Helicobacter and Pasteurella Pneumotropica free conditions at the Massachusetts General Hospital all others were bred and maintained under SPF conditions. Male and female mice were used at 6-12 weeks. All procedures were approved and carried out according to the standards and guidelines set forth by the Institutional Animal Care and Use Committee of Massachusetts General Hospital.
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10

Murine C57BL/6J and Thy1.1 Experiments

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Female C57BL/6J mice aged 6–12 weeks were used for all experiments. WT mice were purchased from Daehan Bio Link (Eumsung, Republic of Korea). Thy1.1 mice were purchased from The Jackson Laboratory (Bar Harbor, ME, USA). All mice were housed under specific pathogen-free conditions, and all animal experiments were approved by the Sogang University Institutional Animal Care and Use Committee (approval no. IACUCSGU2019_09).
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